A Clinical Study to Evaluate the Safety and Tolerability of AWT020 in Patients With Advanced Malignancies

The purpose of this phase I clinical study was to evaluate the safety and tolerability of AWT020 monotherapy and combination with other antitumor therapies in patients with advanced malignancies

Trial Details

NCT ID
NCT06839105
Phase
PHASE1
Sponsor
Shanghai Junshi Bioscience Co., Ltd.
Status
RECRUITING
Cancer Type
Adenocarcinoma Lung Cancer
Interventions
  • Taxol
  • Cisplatin or Carboplatin
  • Pemetrexed
  • Oxaliplatin
  • Capecitabine
  • Bevacizumab
Locations (sample)
  • Fuzhou, Fujian, China|26.06139,119.30611
  • Guangzhou, Guangdong, China|23.11667,113.25
  • Harbin, Heilongjiang, China|45.75,126.65
  • Luoyang, Henan, China|34.67345,112.43684
  • Wuhan, Hubei, China|30.58333,114.26667

Key Eligibility Criteria

  • Both male and female subjects who are at least 18 years old at the time of signing the consent form;
  • Inclusion of patients with advanced malignancies confirmed histologically or cytologically and meeting the following requirements:
  • Single-agent dose escalation and expansion phase to include patients with advanced malignant tumors who have failed or are intolerant of standard t…
  • Therapeutic effect expansion stage of single drug:

For full eligibility, visit ClinicalTrials.gov.

Check If You May Be Eligible

Trialify translates complex eligibility criteria into plain yes-or-no questions to help you understand if this trial might be right for you.

Find Adenocarcinoma Lung Cancer Trials on Trialify →